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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716618Generated: October 26, 2026

Ethanolamine → Benzoic acid, 3-(6-amino-3-methyl-2-pyridinyl)-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/716618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantPyridineHCID 1049—
ReactantMethanesulfonic anhydrideHCID 81560—
Reactant2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 58488371—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductBenzoic acid, 3-(6-amino-3-methyl-2-pyridinyl)-, 1,1-dimethylethyl esterHCID 4548051753%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of 2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide (1 eq) and pyridine (4 eq) in MeCN (8 vol) is heated to 70° C. A solution of methanesulfonic anhydride (1.5 eq) in MeCN (2 vol) is added over 50 min via addition funnel maintaining the temperature at less than 75° C. The mixture is stirred for an additional 0.5 hours after complete addition. The mixture is then allowed to cool to ambient. Ethanolamine (10 eq) is added via addition funnel. After stirring for 2 hours, water (6 vol) is added and the mixture is cooled to 10° C. After stirring for NLT 3 hours, the solid is collected by filtration and washed with water (3 vol), 2:1 MeCN/water (3 vol), and MeCN (2×1.5 vol). The solid is dried to constant weight (<1% difference) in a vacuum oven at 50° C. with a slight N2 bleed to afford tert-butyl-3-(6-amino-3-methylpyridin-2-yl)benzoate as a red-yellow solid (53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09192606B2
Source datasetuspto-grants-2015_11
ORD IDord-3698b297500f4be591d093a8118fb597
Source noteuspto-grants-2015_11